Leucoplast Isolation and Subfractionation

Methods Mol Biol. 2017:1511:73-81. doi: 10.1007/978-1-4939-6533-5_6.

Abstract

Leucoplasts are colorless plastids of nonphotosynthetic plant tissues that support a variety of anabolic roles, particularly the biosynthesis of long-chain fatty acids in storage tissues of developing oil seeds. They also perform other important metabolic functions including the biosynthesis of amino acids and tetrapyrrole compounds. Leucoplasts use a complex set of membrane carriers and channels to actively translocate nuclear-encoded precursor proteins from the cytosol, while exchanging various metabolites with the cytosol. Leucoplast purification is a necessary prerequisite for detailed studies of their soluble (stromal) and membrane (envelope) (phospho)proteomes, as well as for achieving a detailed understanding of their metabolic capabilities, transport processes, and biogenesis. This chapter describes protocols for leucoplast purification from endosperm of developing castor oil seeds, and their subsequent subfractionation into envelope membrane and soluble stromal compartments for biochemical analysis.

Keywords: Castor oil seeds; Cell fractionation; Envelope membranes; Percoll density gradients; Stroma.

MeSH terms

  • Active Transport, Cell Nucleus
  • Cell Fractionation / instrumentation
  • Cell Fractionation / methods*
  • Cell Nucleus / chemistry*
  • Cell Nucleus / ultrastructure
  • Centrifugation, Density Gradient / instrumentation
  • Centrifugation, Density Gradient / methods
  • Culture Media / chemistry
  • Endosperm / chemistry
  • Intracellular Membranes / chemistry*
  • Intracellular Membranes / ultrastructure
  • Plant Proteins / chemistry
  • Plant Proteins / isolation & purification*
  • Plastids / chemistry*
  • Plastids / ultrastructure
  • Povidone / chemistry
  • Protein Transport
  • Ricinus communis / chemistry*
  • Silicon Dioxide / chemistry

Substances

  • Culture Media
  • Plant Proteins
  • Percoll
  • Silicon Dioxide
  • Povidone